null

SMILES COc1cccc(COc2cc(cc(c2)C(O)=O)N2CC(CC2=O)c2ccc(OC)c(OC3CCCC3)c2)c1

InChI Key InChIKey=UQHGEVKJBWBSGG-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50450772   

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(RAT)
Novartis Horsham Research Center

Curated by ChEMBL
LigandPNGBDBM50450772(CHEMBL322092)copy SMILEScopy InChI
Affinity DataIC50: 7.70nMAssay Description:Inhibition of phosphodiesterase (PDE) 4BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZS2Z11PubMed
TargetcGMP-inhibited 3',5'-cyclic phosphodiesterase 3A/3B(Homo sapiens (Human))
Novartis Horsham Research Center

Curated by ChEMBL
LigandPNGBDBM50450772(CHEMBL322092)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of phosphodiesterase (PDE) 3More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZS2Z11PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4D(Homo sapiens (Human))
Novartis Horsham Research Center

Curated by ChEMBL
LigandPNGBDBM50450772(CHEMBL322092)copy SMILEScopy InChI
Affinity DataIC50: 7.90nMAssay Description:Inhibition of phosphodiesterase (PDE) 4DMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZS2Z11PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A(Homo sapiens (Human))
Novartis Horsham Research Center

Curated by ChEMBL
LigandPNGBDBM50450772(CHEMBL322092)copy SMILEScopy InChI
Affinity DataIC50: 7.90nMAssay Description:Inhibition of phosphodiesterase (PDE) 4AMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZS2Z11PubMed